医学
阿尔波特综合征
免疫学
肾小球肾炎
内科学
肾
作者
Nanette Clare,Milka M. Montiel,Meyer D. Lifschitz,George A. Bannayan
出处
期刊:American Journal of Clinical Pathology
[Oxford University Press]
日期:1979-07-01
卷期号:72 (1): 111-117
被引量:42
标识
DOI:10.1093/ajcp/72.1.111
摘要
The combined occurrence of hereditary nephritis with nerve deafness (Alport’s syndrome) and macrothrombocytopathic thrombocytopenia is very rare. The authors have had the opportunity to study such a case in a 20-year-old man who had been followed since birth. The clinical history, renal biopsy, platelet studies, and autopsy findings are presented. The renal pathologic findings are well defined; however, the hemostatic abnormalities and the hearing loss are not well characterized. In this paper, an attempt is made to clarify the diverse platelet functional and morphologic abnormalities.
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